protein
| interacts with MAD2L1 |
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although MAD2L1BP binds to MAD2L1, it promotes the dissociation of CDC20 from BUB1B in MCC  |
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binding of MAD2L1BP to MAD2L1 in mitotic checkpoint complex (MCC) may trigger a conformational change in CDC20 that facilitates its phosphorylation by CDK, and the latter process may promote its dissociation from BUB1B  |
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is a well-known interacting partner of the spindle assembly checkpoint (SAC) effector molecule MAD2L1  |
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promotes efficient mitotic exit, specifically the metaphase-anaphase transition, by antagonizing MAD2L1 function  |
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is an antagonist of the SAC effector MAD2L1 and promotes silencing of the SAC and mitotic progression  |
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TRIP13, aided by the adapter protein MAD2L1BP, converts the HORMA-family spindle checkpoint protein MAD2L1 from a signaling-active 'closed' conformer to an inactive 'open' conformer  |
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TRIP13, jointly with the MAD2L1BP, promotes the inactivation of the mitotic (spindle assembly) checkpoint by disassembling the mitotic checkpoint complex (MCC)  |
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MAD2L1BP-induced cell death is mediated by interactions with MAD2L1 that lead to its inactivation is potentially applicable in anticancer therapy |
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MAD2L1 inhibitory protein MAD2L1BP promotes checkpoint inactivation and timely chromosome segregation  |
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MAD2L1BP blocks the MAD2L1-BUB1B interaction and prevents spontaneous clathrin-mediated INSR endocytosis  |
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MAD2L1BP binding to the TRIP13 N-terminal domain positions the disordered MAD2L1 N-terminus for engagement by the TRIP13 "pore loops", which in cells causes spindle assembly checkpoint defects consistent with loss of TRIP13 function  |
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TRIP13-MAD2L1BP intercepts and disassembles free MCC not bound to anaphase-promoting complex/cyclosome (APC/C) through mediating the local unfolding of the MAD2L1 C-terminal region  |